Black cartilage: Incidentally discovered articular ochronosis during arthroplasty von Kumps, Camille, Stanovici, Julien, Chaibi, Emmelie, Campos‐Xavier, Belinda, Pavlidou, Despina Christina, Tran, Christel

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Efficient Estimation of Data Combination Models by the Method of Auxiliary-to-Study Tilting (AST) von Graham, Bryan S., Pinto, Cristine Campos de Xavier, Egel, Daniel

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Inverse Probability Tilting for Moment Condition Models with Missing Data von GRAHAM, BRYAN S., DE XAVIER PINTO, CRISTINE CAMPOS, EGEL, DANIEL

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Modeling land cover change based on an artificial neural network for a semiarid river basin in northeastern Brazil von Silva, Leonardo Pereira e, Xavier, Ana Paula Campos, da Silva, Richarde Marques, Santos, Celso Augusto Guimarães

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Recurrent Increased Nuchal Translucency Led to the Identification of Novel NUP107 Variants von Atallah, Isis, Cisarova, Katarina, Guenot, Cécile, Dubruc, Estelle, Superti-Furga, Andrea, Campos-Xavier, Belinda, Unger, Sheila

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A monoallelic SEC23A variant E599K associated with cranio‐lenticulo‐sutural dysplasia von Cisarova, Katarina, Garavelli, Livia, Caraffi, Stefano Giuseppe, Peluso, Francesca, Valeri, Lara, Gargano, Giancarlo, Gavioli, Sara, Trimarchi, Gabriele, Neri, Alberto, Campos‐Xavier, Belinda, Superti‐Furga, Andrea

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Chondrodysplasia and growth failure in children after early hematopoietic stem cell transplantation for non‐oncologic disorders von Botto, Lorenzo D., Meeths, Marie, Campos‐Xavier, Belinda, Bergamaschi, Rosalba, Mazzanti, Laura, Scarano, Emanuela, Finocchi, Andrea, Cancrini, Caterina, Zirn, Birgit, Kühnle, Ingrid, Kramm, Christof Maria, Alanay, Yasemin, Jones, Wendy D., Irving, Melita, Sabir, Ataf, Henter, Jan‐Inge, Borgström, Birgit, Nordgren, Ann, Hammarsjö, Anna, Putti, Caterina, Mozzato, Chiara, Zuccarello, Daniela, Nishimura, Gen, Bonafè, Luisa, Grigelioniene, Giedre, Unger, Sheila, Superti‐Furga, Andrea

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NBAS mutations cause a multisystem disorder involving bone, connective tissue, liver, immune system, and retina von Segarra, Nuria Garcia, Ballhausen, Diana, Crawford, Heather, Perreau, Matthieu, Campos-Xavier, Belinda, van Spaendonck-Zwarts, Karin, Vermeer, Cees, Russo, Michel, Zambelli, Pierre-Yves, Stevenson, Brian, Royer-Bertrand, Beryl, Rivolta, Carlo, Candotti, Fabio, Unger, Sheila, Munier, Francis L., Superti-Furga, Andrea, Bonafé, Luisa

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Immune deficiency, autoimmune disease and intellectual disability: A pleiotropic disorder caused by biallelic variants in the TPP2 gene von Atallah, Isis, Quinodoz, Mathieu, Campos‐Xavier, Belinda, Peter, Virginie G., Fouriki, Athina, Bonvin, Christophe, Bottani, Armand, Kumps, Camille, Angelini, Federica, Bellutti Enders, Felicitas, Christen‐Zaech, Stéphanie, Rizzi, Mattia, Renella, Raffaele, Beck‐Popovic, Maja, Poloni, Claudia, Frossard, Valérie, Blouin, Jean‐Louis, Rivolta, Carlo, Riccio, Orbicia, Candotti, Fabio, Hofer, Michael, Unger, Sheila, Superti‐Furga, Andrea

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Mutations in LONP1, a mitochondrial matrix protease, cause CODAS syndrome von Dikoglu, Esra, Alfaiz, Ali, Gorna, Maria, Bertola, Deborah, Chae, Jong Hee, Cho, Tae-Joon, Derbent, Murat, Alanay, Yasemin, Guran, Tulay, Kim, Ok-Hwa, Llerenar Jr, Juan C., Yamamoto, Guillerme, Superti-Furga, Giulio, Reymond, Alexandre, Xenarios, Ioannis, Stevenson, Brian, Campos-Xavier, Belinda, Bonafé, Luisa, Superti-Furga, Andrea, Unger, Sheila

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Identification of novel LFNG mutations in spondylocostal dysostosis von Otomo, Nao, Mizumoto, Shuji, Lu, Hsing-Fang, Takeda, Kazuki, Campos-Xavier, Belinda, Mittaz-Crettol, Lauréane, Guo, Long, Takikawa, Kazuharu, Nakamura, Masaya, Yamada, Shuhei, Matsumoto, Morio, Watanabe, Kota, Ikegawa, Shiro

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Mutations in the Heparan-Sulfate Proteoglycan Glypican 6 (GPC6) Impair Endochondral Ossification and Cause Recessive Omodysplasia von Campos-Xavier, Ana Belinda, Martinet, Danielle, Bateman, John, Belluoccio, Dan, Rowley, Lynn, Tan, Tiong Yang, Baxová, Alica, Gustavson, Karl-Henrik, Borochowitz, Zvi U., Innes, A. Micheil, Unger, Sheila, Beckmann, Jacques S., Mittaz, Lauréane, Ballhausen, Diana, Superti-Furga, Andrea, Savarirayan, Ravi, Bonafé, Luisa

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Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies von Machol, Keren, Jain, Mahim, Almannai, Mohammed, Orand, Thibault, Lu, James T., Tran, Alyssa, Chen, Yuqing, Schlesinger, Alan, Gibbs, Richard, Bonafe, Luisa, Campos‐Xavier, Ana Belinda, Unger, Sheila, Superti‐Furga, Andrea, Lee, Brendan H., Campeau, Philippe M., Burrage, Lindsay C.

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Confirmation of spondylo‐epi‐metaphyseal dysplasia with joint laxity, EXOC6B type von Campos‐Xavier, Belinda, Rogers, R. Curtis, Niel‐Bütschi, Florence, Ferreira, Catarina, Unger, Sheila, Spranger, Jürgen, Superti‐Furga, Andrea

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Efficacy and Safety of Femtosecond Laser-Assisted Cataract Surgery Compared with Manual Cataract Surgery: A Meta-Analysis of 14 567 Eyes von Popovic, Marko, Campos-Möller, Xavier, Schlenker, Matthew B, Ahmed, Iqbal Ike K

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Phenotypic and molecular characterization of Bruck syndrome (osteogenesis imperfecta with contractures of the large joints) caused by a recessive mutation in PLOD2 von Ha-Vinh, Russia, Alanay, Yasemin, Bank, Ruud A., Campos-Xavier, Ana Belinda, Zankl, Andreas, Superti-Furga, Andrea, Bonafé, Luisa

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Post-axial polydactyly type A2, overgrowth and autistic traits associated with a chromosome 13q31.3 microduplication encompassing miR-17-92 and GPC5 von Kannu, P, Campos-Xavier, A.B, Hull, D, Martinet, D, Ballhausen, D, Bonafé, L

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Brief Report: Peripheral Osteolysis in Adults Linked to ASAH1 (Acid Ceramidase) Mutations: A New Presentation of Farber's Disease von Bonafé, Luisa, Kariminejad, Ariana, Li, Jia, Royer‐Bertrand, Beryl, Garcia, Virginie, Mahdavi, Shokouholsadat, Bozorgmehr, Bita, Lachman, Ralph L., Mittaz‐Crettol, Lauréane, Campos‐Xavier, Belinda, Nampoothiri, Sheela, Unger, Sheila, Rivolta, Carlo, Levade, Thierry, Superti‐Furga, Andrea

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Positive effects of an angiotensin II type 1 receptor antagonist in Camurati-Engelmann disease: A single case observation von Simsek-Kiper, Pelin Ozlem, Dikoglu, Esra, Campos-Xavier, Belinda, Utine, Gulen Eda, Bonafe, Luisa, Unger, Sheila, Boduroglu, Koray, Superti-Furga, Andrea

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Intraocular lens power calculation in primary angle closure von Campos-Möller, Xavier, Ike K Ahmed, Iqbal

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